Stroke, Vol 24, 1083-1086, Copyright © 1993 by American Heart Association
N Tanahashi, Y Fukuuchi, M Tomita, S Matsuoka and H Takeda
BACKGROUND AND PURPOSE: We examined the effect of ticlopidine hydrochloride
on the enhanced erythrocyte aggregability in 14 patients with cerebral
infarction during the chronic phase (over 1 month after onset). SUMMARY OF
REPORT: Ticlopidine (100 mg BID) was administered for 8 weeks. We measured
the rate of erythrocyte aggregation (aggregability), using the whole-blood
erythrocyte aggregometer that we developed, before and at 4 and 8 weeks
after the initiation of ticlopidine administration. Concomitant
measurements were made of such blood factors as the hematocrit,
albumin-globulin ratio, and fibrinogen concentration. The erythrocyte
aggregation rates before and at 4 and 8 weeks after were 0.147 +/- 0.017/s,
0.138 +/- 0.019/s, and 0.133 +/- 0.017/s, respectively. The erythrocyte
aggregation rates at 4 and 8 weeks were significantly lower (P < .05 by
Bonferroni's modified t test) than those before ticlopidine administration.
At 4 and 8 weeks after the initiation of ticlopidine treatment, the
hematocrit value and concentration of fibrinogen were also significantly (P
< .05) reduced. CONCLUSIONS: Our results suggest that ticlopidine can
improve the enhanced erythrocyte aggregability in patients with cerebral
infarction during the chronic phase.
ARTICLES
Ticlopidine improves the enhanced erythrocyte aggregability in patients with cerebral infarction
Department of Neurology, School of Medicine, Keio University, Tokyo, Japan.
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